US9102659B2 - Multifunctional nitroxide derivatives and uses thereof - Google Patents
Multifunctional nitroxide derivatives and uses thereof Download PDFInfo
- Publication number
- US9102659B2 US9102659B2 US13/992,396 US201113992396A US9102659B2 US 9102659 B2 US9102659 B2 US 9102659B2 US 201113992396 A US201113992396 A US 201113992396A US 9102659 B2 US9102659 B2 US 9102659B2
- Authority
- US
- United States
- Prior art keywords
- guanidine
- hydroxy
- cyano
- compound
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical class ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 title abstract description 62
- 150000001875 compounds Chemical class 0.000 claims abstract description 113
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 27
- -1 —OH Chemical group 0.000 claims description 95
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 37
- 239000000203 mixture Substances 0.000 claims description 30
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 26
- 150000003839 salts Chemical class 0.000 claims description 23
- 125000004432 carbon atom Chemical group C* 0.000 claims description 21
- 229910052801 chlorine Inorganic materials 0.000 claims description 21
- 125000001424 substituent group Chemical group 0.000 claims description 19
- 229910052736 halogen Inorganic materials 0.000 claims description 18
- 150000002367 halogens Chemical group 0.000 claims description 18
- 229910052794 bromium Inorganic materials 0.000 claims description 14
- 125000000623 heterocyclic group Chemical group 0.000 claims description 14
- 229910052731 fluorine Inorganic materials 0.000 claims description 12
- 239000012453 solvate Substances 0.000 claims description 12
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 10
- 125000001072 heteroaryl group Chemical group 0.000 claims description 9
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 7
- 125000001054 5 membered carbocyclic group Chemical group 0.000 claims description 7
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 5
- 239000000725 suspension Substances 0.000 claims description 5
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 4
- NJRZGXLLFIJSBG-UHFFFAOYSA-N 1-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)-3-pyridin-3-ylguanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=CN=C1 NJRZGXLLFIJSBG-UHFFFAOYSA-N 0.000 claims description 4
- 125000005915 C6-C14 aryl group Chemical group 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 4
- CWMPXOXZIFRGST-UHFFFAOYSA-N 1-(6-chloropyridin-3-yl)-3-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=C(Cl)N=C1 CWMPXOXZIFRGST-UHFFFAOYSA-N 0.000 claims description 3
- GKQGFZBFFZPSTC-UHFFFAOYSA-N 1-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)-3-pyridin-4-ylguanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=NC=C1 GKQGFZBFFZPSTC-UHFFFAOYSA-N 0.000 claims description 3
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- ZYEXYAFUENXJAJ-UHFFFAOYSA-N 1-(2-bromopyridin-3-yl)-3-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=CN=C1Br ZYEXYAFUENXJAJ-UHFFFAOYSA-N 0.000 claims description 2
- UWHYEZMCECCXTQ-UHFFFAOYSA-N 1-(2-bromopyridin-4-yl)-3-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=NC(Br)=C1 UWHYEZMCECCXTQ-UHFFFAOYSA-N 0.000 claims description 2
- VUYCYGWCUJCEJH-UHFFFAOYSA-N 1-(2-chloropyridin-3-yl)-3-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=CN=C1Cl VUYCYGWCUJCEJH-UHFFFAOYSA-N 0.000 claims description 2
- QIWSEYFCQJPRRO-UHFFFAOYSA-N 1-(2-chloropyridin-4-yl)-3-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=NC(Cl)=C1 QIWSEYFCQJPRRO-UHFFFAOYSA-N 0.000 claims description 2
- GTUDUGCFKZZQFE-UHFFFAOYSA-N 1-(6-bromopyridin-2-yl)-3-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=CC(Br)=N1 GTUDUGCFKZZQFE-UHFFFAOYSA-N 0.000 claims description 2
- FPBQUIZCDPOEBS-UHFFFAOYSA-N 1-(6-bromopyridin-3-yl)-3-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=C(Br)N=C1 FPBQUIZCDPOEBS-UHFFFAOYSA-N 0.000 claims description 2
- DEDQNWORFCDNJG-UHFFFAOYSA-N 1-(6-chloropyridin-2-yl)-3-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=CC(Cl)=N1 DEDQNWORFCDNJG-UHFFFAOYSA-N 0.000 claims description 2
- LKNJWTIXBSWCRJ-UHFFFAOYSA-N 1-cyano-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)-3-pyridin-2-ylguanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=CC=N1 LKNJWTIXBSWCRJ-UHFFFAOYSA-N 0.000 claims description 2
- LXCWNBUIPNFJKD-UHFFFAOYSA-N 1-cyano-3-(2-fluoropyridin-3-yl)-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=CN=C1F LXCWNBUIPNFJKD-UHFFFAOYSA-N 0.000 claims description 2
- VASYICCMKZGOHN-UHFFFAOYSA-N 1-cyano-3-(2-fluoropyridin-4-yl)-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=NC(F)=C1 VASYICCMKZGOHN-UHFFFAOYSA-N 0.000 claims description 2
- HMAARCCBGHVWQW-UHFFFAOYSA-N 1-cyano-3-(6-fluoropyridin-3-yl)-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)N(O)C(C)(C)CC1NC(=NC#N)NC1=CC=C(F)N=C1 HMAARCCBGHVWQW-UHFFFAOYSA-N 0.000 claims description 2
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 2
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- RGAMYZQGEQHZAH-UHFFFAOYSA-N 1-cyano-3-(6-fluoropyridin-2-yl)-2-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine Chemical compound CC1(C)CC(NC(Nc2cccc(F)n2)=NC#N)C(C)(C)N1O RGAMYZQGEQHZAH-UHFFFAOYSA-N 0.000 claims 1
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Definitions
- R 3 each independently is selected from (C 1 -C 8 )alkyl, (C 2 -C 8 )alkenyl, or (C 2 -C 8 )alkynyl;
- the multifunctional nitroxide derivatives and pharmaceutical compositions of the invention are useful for treatment, prevention and/or managing of diseases, disorders and conditions associated with high levels of reactive oxygen species (ROS) and oxidative stress.
- ROS reactive oxygen species
- the present invention provides a multifunctional nitroxide derivative of the general formula I as defined above, or an enantiomer, diastereomer, racemate, or a pharmaceutically acceptable salt, solvate or prodrug thereof, for use in treatment of a disease, disorder or condition associated with high levels of ROS, and oxidative stress.
- FIG. 1 shows the mean arterial pressure (mmHg) measured in rats subjected to a model of myocardial ischemia-reperfusion (I/R) injury (MIRI) as described in Example 11, indicating that compound 2, when administered prior to reperfusion at 1 mg/kg IV bolus followed by a continuous IV infusion of 2 mg/kg/h, did not produce systemic hypotension.
- MIRI myocardial ischemia-reperfusion
- alkylene typically means a divalent straight or branched hydrocarbon radical having 1-8 carbon atoms and includes, e.g., methylene, ethylene, propylene, butylene, 2-methylpropylene, pentylene, 2-methylbutylene, hexylene, 2-methylpentylene, 3-methylpentylene, 2,3-dimethylbutylene, heptylene, octylene and the like.
- the multifunctional nitroxide derivative of the present invention is a compound of the general formulas Ia-1 to Ia-9, a compound of the general formula Ib-1 to Ib-3, or a compound of the general formula Ic-1 to Ic-9, wherein R 4 is H.
- the multifunctional nitroxide derivative of the invention is a compound of the general formula I, wherein Y is CH; X is absent; R 2 is H; R 3 is methyl; and R 1 is F, Cl or Br, linked to the phenyl ring at position ortho, meta or para with respect to A, i.e., the oxy radical of 2-cyano-1-(2-fluoro phenyl)-3-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine, 2-cyano-1-(2-chlorophenyl)-3-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl)guanidine, or 2-cyano-1-(2-bromophenyl)-3-(1-hydroxy-2,2,5,5-tetramethylpyrrolidin-3-yl) guanidine (compounds 23 a -23 c , respectively); 2-cyano-1-(3-fluorophenyl)-3
- compound 2 significantly reduced both myocardial myeloperoxidase (MPO) ( 2 A) and tissue infarction ( 2 B).
- MPO myocardial myeloperoxidase
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| PCT/IL2011/000931 WO2012077108A1 (en) | 2010-12-09 | 2011-12-08 | Multifunctional nitroxide derivatives and uses thereof |
| US13/992,396 US9102659B2 (en) | 2010-12-09 | 2011-12-08 | Multifunctional nitroxide derivatives and uses thereof |
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| US15/384,094 Abandoned US20170107198A1 (en) | 2010-12-09 | 2016-12-19 | Multifunctional nitroxide derivatives and uses thereof |
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| US15/384,094 Abandoned US20170107198A1 (en) | 2010-12-09 | 2016-12-19 | Multifunctional nitroxide derivatives and uses thereof |
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| AU2014224249B2 (en) * | 2013-03-05 | 2017-10-05 | Salzman Group Pty. Ltd | Prodrugs of multifunctional nitroxide derivatives and uses thereof |
| JP6557977B2 (ja) * | 2015-01-15 | 2019-08-14 | Jnc株式会社 | 含窒素環化合物を含有する液晶組成物および液晶表示素子 |
| WO2017208129A1 (en) | 2016-05-31 | 2017-12-07 | Tisbury Pharmaceuticals, Inc. | Pharmaceutical composition and method for reducing intraocular pressure |
| CN111630048B (zh) * | 2018-03-19 | 2023-09-29 | 四川科伦博泰生物医药股份有限公司 | 脒类和胍类衍生物、其制备方法及其在医药上的应用 |
| WO2021044413A1 (en) * | 2019-09-03 | 2021-03-11 | Salzman Group Ltd. | Atp-regulated potassium channel openers comprising guanidine and uses thereof |
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| US5011837A (en) | 1988-08-09 | 1991-04-30 | E. R. Squibb & Sons, Inc. | Aryl cyanoguanidines: potassium channel activators and method of making same |
| WO2004000331A1 (en) | 2002-06-21 | 2003-12-31 | Global Cardiac Solutions Pty Ltd | Organ arrest, protection, preservation and recovery |
| US20060025446A1 (en) | 2004-07-27 | 2006-02-02 | Jeffrey Sterling | Propargyl nitroxides and indanyl nitroxides and their use for the treatment of neurologic diseases and disorders |
| US8202852B2 (en) * | 2006-06-06 | 2012-06-19 | Xenoport, Inc. | Creatine phosphate analog prodrugs, compositions and uses thereof |
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| US2A (en) * | 1826-12-15 | 1836-07-29 | John Goulding | Mode of manufacturing wool or other fibrous materials |
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| US5374643A (en) * | 1992-09-11 | 1994-12-20 | E. R. Squibb & Sons, Inc. | Aryl urea (thiourea) and cyanoguanidine derivatives |
| DE69534341T2 (de) * | 1994-12-12 | 2006-05-24 | Omeros Corp., Seattle | Bespüllungslösung und deren verwendung zur perioperativen hemmung von schmerzen, entzündungen und spasmen an einer wunde |
| AU760174B2 (en) * | 1999-02-09 | 2003-05-08 | Bristol-Myers Squibb Company | Lactam inhibitors of FXa and method |
| IL158574A0 (en) * | 2001-05-24 | 2004-05-12 | Leo Pharma As | Novel pyridyl cyanoguanidine compounds |
| WO2004078172A2 (en) * | 2003-03-06 | 2004-09-16 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Sod mimic multifunctional compounds for treating inflammatory bowel disease |
| CN1854135B (zh) * | 2005-04-18 | 2013-06-12 | 李伟章 | 由氰基胍连接组成的杂环化合物及其医药应用 |
| US20070275944A1 (en) * | 2006-04-05 | 2007-11-29 | The Board Of Trustees Operating Michigan State University | Antioxidants and methods of their use |
| CA2707158A1 (en) * | 2007-11-28 | 2009-06-04 | Revision Therapeutics, Inc. | Modulators of ocular oxidative stress |
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2011
- 2011-12-08 HR HRP20160747TT patent/HRP20160747T1/hr unknown
- 2011-12-08 ES ES11808945.7T patent/ES2580104T3/es active Active
- 2011-12-08 SI SI201130873A patent/SI2649048T1/sl unknown
- 2011-12-08 US US13/992,396 patent/US9102659B2/en not_active Expired - Fee Related
- 2011-12-08 RU RU2013126219/04A patent/RU2597265C2/ru not_active IP Right Cessation
- 2011-12-08 EP EP11808945.7A patent/EP2649048B1/en active Active
- 2011-12-08 WO PCT/IL2011/000931 patent/WO2012077108A1/en not_active Ceased
- 2011-12-08 JP JP2013542666A patent/JP5853030B2/ja not_active Expired - Fee Related
- 2011-12-08 CN CN201180067011.6A patent/CN103347856B/zh not_active Expired - Fee Related
- 2011-12-08 DK DK11808945.7T patent/DK2649048T3/en active
- 2011-12-08 PT PT118089457T patent/PT2649048T/pt unknown
- 2011-12-08 RS RS20160494A patent/RS54889B1/sr unknown
- 2011-12-08 PL PL11808945.7T patent/PL2649048T3/pl unknown
- 2011-12-08 CA CA2820763A patent/CA2820763A1/en not_active Abandoned
- 2011-12-08 HU HUE11808945A patent/HUE029466T2/en unknown
- 2011-12-08 AU AU2011340037A patent/AU2011340037B2/en not_active Ceased
- 2011-12-08 BR BR112013014190A patent/BR112013014190A2/pt active Search and Examination
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2015
- 2015-07-31 US US14/815,783 patent/US9522903B2/en not_active Expired - Fee Related
-
2016
- 2016-12-19 US US15/384,094 patent/US20170107198A1/en not_active Abandoned
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| US5011837A (en) | 1988-08-09 | 1991-04-30 | E. R. Squibb & Sons, Inc. | Aryl cyanoguanidines: potassium channel activators and method of making same |
| WO2004000331A1 (en) | 2002-06-21 | 2003-12-31 | Global Cardiac Solutions Pty Ltd | Organ arrest, protection, preservation and recovery |
| US20060025446A1 (en) | 2004-07-27 | 2006-02-02 | Jeffrey Sterling | Propargyl nitroxides and indanyl nitroxides and their use for the treatment of neurologic diseases and disorders |
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Also Published As
| Publication number | Publication date |
|---|---|
| PL2649048T3 (pl) | 2016-10-31 |
| US20150336932A1 (en) | 2015-11-26 |
| HRP20160747T1 (hr) | 2016-09-23 |
| US9522903B2 (en) | 2016-12-20 |
| HUE029466T2 (en) | 2017-02-28 |
| SI2649048T1 (sl) | 2016-10-28 |
| US20170107198A1 (en) | 2017-04-20 |
| RU2013126219A (ru) | 2015-01-20 |
| EP2649048A1 (en) | 2013-10-16 |
| US20130338146A1 (en) | 2013-12-19 |
| RS54889B1 (sr) | 2016-10-31 |
| RU2597265C2 (ru) | 2016-09-10 |
| JP2013544880A (ja) | 2013-12-19 |
| CA2820763A1 (en) | 2012-06-14 |
| JP5853030B2 (ja) | 2016-02-09 |
| AU2011340037A1 (en) | 2013-07-04 |
| DK2649048T3 (en) | 2016-07-25 |
| CN103347856B (zh) | 2016-03-09 |
| AU2011340037B2 (en) | 2016-03-17 |
| PT2649048T (pt) | 2016-07-13 |
| BR112013014190A2 (pt) | 2016-09-13 |
| CN103347856A (zh) | 2013-10-09 |
| EP2649048B1 (en) | 2016-03-30 |
| ES2580104T3 (es) | 2016-08-19 |
| WO2012077108A1 (en) | 2012-06-14 |
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